Chain extension study of aqueous polyurethane dispersions

被引:167
作者
Jhon, YK [1 ]
Cheong, IW [1 ]
Kim, JH [1 ]
机构
[1] Yonsei Univ, Dept Chem Engn, Nanosphere Proc & Technol Lab, Seodaemoon Ku, Seoul 120749, South Korea
关键词
polyurethane dispersions; chain extension; weight average molecular weights; residual NCO group; adhesive strength;
D O I
10.1016/S0927-7757(00)00714-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In the several decades, aqueous polyurethane dispersion has been investigated by many researchers. However, relatively little systematic work has been reported in detail on chain extension process. This work describes the reaction of chain extension step (chain extended reaction) as the variation of residual NCO group and subsequent weight average molecular weight of the polyurethane during the chain extension step. Polyurethane dispersion was prepared by neutralization emulsification method. The dispersions with prepared different average particle sizes were obtained by varying the degree of neutralization and each of them chain extended subsequently by water-soluble chain extender: 1,6-hexanediamine. Time-dependent change of fret: and residual NCO group was measured by FT-IR spectroscopy during the chain extension process. As the total surface area of polyurethane particle decreased, the amount of residual NCO group and consequently required amount chain extender for optimum chain extension decreased. According to the GPC and FT-IR data, optimum amount of 1,6-hexanediamine was determined by the location of the NCO group and contact area between the residual NCO groups and water molecules. Additionally, it was found that excess amount of chain extender had an unfavorable influence on adhesive strength. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:71 / 78
页数:8
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